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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR1900024985 |
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最近更新日期: Date of Last Refreshed on: |
2019-08-06 11:17:51 |
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注册时间: Date of Registration: |
2019-08-06 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
李想医师:该研究尚未获得伦理委员会批准。请于批准后再开始纳入参试者,并与我们联系上传批件。 联合应用利伐沙班和氨甲环酸用于脊柱手术的出血和血栓管理研究 |
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Public title: |
Combined use of rivaroxaban and tranexamic acid for hemorrhage and thrombosis management in spine surgery |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
联合应用利伐沙班和氨甲环酸用于脊柱手术的出血和血栓管理研究 |
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Scientific title: |
Combined use of rivaroxaban and tranexamic acid for hemorrhage and thrombosis management in spine surgery |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
李想 |
研究负责人: |
陈允震 |
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Applicant: |
Xiang Li |
Study leader: |
Yunzhen Chen |
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申请注册联系人电话: Applicant telephone: |
+86 13573101270 |
研究负责人电话:
Study leader's |
+86 18560082566 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
sddxqlyylx@163.com |
研究负责人电子邮件: Study leader's E-mail: |
qilucyz@yeah.net |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
山东省济南市历下区文化西路107号山东大学齐鲁医院骨外一科 |
研究负责人通讯地址: |
山东省济南市历下区文化西路107号山东大学齐鲁医院骨外一科 |
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Applicant address: |
107 Wenhua Road West, Lixia District, Ji'nan, Shandong, China |
Study leader's address: |
107 Wenhua Road West, Lixia District, Ji'nan, Shandong, China |
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申请注册联系人邮政编码: Applicant postcode: |
250012 |
研究负责人邮政编码: Study leader's postcode: |
250012 |
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申请人所在单位: |
山东大学齐鲁医院 |
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Applicant's institution: |
Department of Orthopedics, Qilu Hospital of Shandong University |
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研究负责人所在单位: |
山东大学齐鲁医院 |
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Affiliation of the Leader: |
Department of Orthopedics, Qilu Hospital of Shandong University |
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是否获伦理委员会批准: |
否 |
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Approved by ethic committee: |
No |
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伦理委员会批件文号: Approved No. of ethic committee: |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
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Name of the ethic committee: |
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伦理委员会批准日期: Date of approved by ethic committee: |
2013-08-26 00:00:00 | ||
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
山东大学齐鲁医院 |
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Primary sponsor: |
Qilu Hospital of Shandong University |
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研究实施负责(组长)单位地址: |
山东省济南市历下区文化西路107号山东大学齐鲁医院骨外一科 |
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Primary sponsor's address: |
Department of Orthopedics, Qilu Hospital of Shandong University, 107 Wenhua West Road, Lixia District, Ji'nan, Shandong, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
自筹 |
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Source(s) of funding: |
self-funded |
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研究疾病: |
静脉血栓栓塞症 |
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Target disease: |
Venous thromboembolism |
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研究疾病代码: |
I80.301 |
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Target disease code: |
I80.301 |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
1、探索氨甲环酸联合用于腰椎后路固定融合手术的用法用量,观察氨甲环酸应用后输血率的变化; 2、观察腰椎后路固定融合术后应用利伐沙班后VTE发生率、引流量和血肿发生率等。 |
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Objectives of Study: |
1. Explore the usage and dosage of tranexamic acid for lumbar posterior fixation fusion surgery, and observe the change of transfusion rate after application of tranexamic acid; 2. Observe the incidence of VTE, drainage and hematoma incidence after the application of rivaroxaban after lumbar posterior fixation fusion. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1.年龄大于18 周岁且小于80 周岁的成年人; |
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Inclusion criteria |
1. Adults aged 18 to 80 years; |
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排除标准: |
1、合并PE或DVT的患者; |
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Exclusion criteria: |
1. Patients with PE or DVT; |
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研究实施时间: Study execute time: |
从 From 2019-09-01 00:00:00至 To 2020-09-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2019-09-01 00:00:00 至 To 2020-09-01 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
患者入院后,首先进行Autar评分,根据评分结果划分至低危组、中高危组,然后由管床医师抽取信封将该患者分入不同的亚组。 李想医师:“信封随机”为错误随机描述方法,请说明何人使用何种方法(随机数字表?统计学软件?或其他)产生随机序列。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
After the patients were admitted to the hospital, the Autar score was first performed. According to the results of the scoring, the patients will be assigned to the low-risk group and the middle-high-risk group. The tube bed physician then take the envelope to divide the patients into different subgroups. |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
单盲 |
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Blinding: |
Single blind |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
是Yes |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
ResMan临床试验公共管理平台, http://www.medresman.org |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Clinical Trial Management Public Platform, http://www.medresman.org |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
ResMan临床试验公共管理平台 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Clinical Trial Management Public Platform |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |